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      Impact of the β1-adrenoceptor Arg389Gly polymorphism on heart-rate responses to bisoprolol and carvedilol in heart-failure patients.

      Clinical Pharmacology and Therapeutics
      Adrenergic beta-1 Receptor Antagonists, administration & dosage, pharmacokinetics, Aged, Atrial Fibrillation, complications, drug therapy, genetics, Bisoprolol, Carbazoles, Dose-Response Relationship, Drug, Double-Blind Method, Female, Heart Failure, Heart Rate, drug effects, Humans, Male, Polymorphism, Single Nucleotide, Propanolamines, Receptors, Adrenergic, beta-1, Treatment Outcome

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          Abstract

          This pharmacogenetic substudy of the prospective, double-blind, randomized CIBIS-ELD trial determined the impact of the β1-adrenoceptor Arg189Gly polymorphism on heart-rate responses to bisoprolol or carvedilol in elderly patients with heart failure (421 with sinus rhythm, 107 with atrial fibrillation). Patients were randomized 1:1 to bisoprolol or carvedilol with a fortnightly dose-doubling scheme and guideline target doses. Patients with sinus rhythm responded essentially identically to bisoprolol and carvedilol, independent of genotype. Atrial fibrillation patients homozygous for Arg389 had a much smaller response to carvedilol than carriers of at least one Gly389 allele (mean difference 12 bpm, P < 0.00001). Carvedilol up to 2 × 12.5 mg did not reduce heart rate in Arg389Arg homozygotes at all. Interestingly, the immediate response to carvedilol did not differ between genotypes. The Arg389Gly polymorphism has a major impact on the heart-rate response to carvedilol (but not bisoprolol) in patients with heart failure plus atrial fibrillation.

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